A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610175



Internal ID16397584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8461340..8591178hg38UCSC Ensembl
Innerchr8:8318850..8448688hg19UCSC Ensembl
Innerchr8:8356260..8486098hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38129839
hg19129839
hg18129839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11939n54
Supporting Variantsnssv1156579, nssv1156580
SamplesHGDP00946, HGDP00112
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610175
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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